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WO2008101659A1 - Dérivés de cyclohexane spirocycliques - Google Patents

Dérivés de cyclohexane spirocycliques Download PDF

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Publication number
WO2008101659A1
WO2008101659A1 PCT/EP2008/001270 EP2008001270W WO2008101659A1 WO 2008101659 A1 WO2008101659 A1 WO 2008101659A1 EP 2008001270 W EP2008001270 W EP 2008001270W WO 2008101659 A1 WO2008101659 A1 WO 2008101659A1
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WIPO (PCT)
Prior art keywords
cyclohexane
amine
hydroxy
unsubstituted
indole
Prior art date
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PCT/EP2008/001270
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German (de)
English (en)
Inventor
Stefan Schunk
Saskia Zemolka
Derek Saunders
Michael Gruss
Heinz Graubaum
Original Assignee
Grünenthal GmbH
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First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=39535309&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO2008101659(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority to CN2008800059845A priority Critical patent/CN101622255B/zh
Priority to PL08707767T priority patent/PL2121689T3/pl
Priority to RU2009135072/04A priority patent/RU2484092C2/ru
Priority to NZ578717A priority patent/NZ578717A/en
Priority to JP2009550239A priority patent/JP5366832B2/ja
Priority to KR1020097019744A priority patent/KR101515795B1/ko
Priority to BRPI0806796-1A priority patent/BRPI0806796A2/pt
Application filed by Grünenthal GmbH filed Critical Grünenthal GmbH
Priority to ES08707767T priority patent/ES2433205T3/es
Priority to MX2009008781A priority patent/MX2009008781A/es
Priority to AU2008217276A priority patent/AU2008217276B2/en
Priority to EP08707767.3A priority patent/EP2121689B1/fr
Priority to HK10103564.8A priority patent/HK1136828B/xx
Priority to CA2679166A priority patent/CA2679166C/fr
Publication of WO2008101659A1 publication Critical patent/WO2008101659A1/fr
Priority to IL200497A priority patent/IL200497A/en
Priority to US12/545,461 priority patent/US8404740B2/en

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    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/10—Spiro-condensed systems
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    • A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/407—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with other heterocyclic ring systems, e.g. ketorolac, physostigmine
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    • C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/10—Spiro-condensed systems
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    • C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/10—Spiro-condensed systems

Definitions

  • the present invention relates to spirocyclic cyclohexane derivatives, processes for their preparation, medicaments containing these compounds and the use of spirocyclic cyclohexane derivatives for the preparation of medicaments.
  • the heptadekapeptide nociceptin is an endogenous ligand of the ORL1 (opioid receptor-like) receptor (Meunier et al., Nature 377, 1995, pp. 532-535), which belongs to the family of opioid receptors and in many regions of the brain and the spinal cord and has a high affinity for the ORL1 receptor.
  • the ORL1 receptor is homologous to the ⁇ , K and ⁇ opioid receptors and the
  • Amino acid sequence of the nociceptin peptide has a strong similarity to those of the known opioid peptides.
  • the induced by nociceptin receptor activation leads via the coupling with G j / O proteins to inhibition of adenylate cyclase (Meunier et al., Nature 377, 1995, pp 532-535).
  • the nociceptin peptide exhibits pronociceptive and hyperalgesic activity in various animal models after intercerebroventular administration (Reinscheid et al., Science 270, 1995, pp. 792-794). These findings can be explained as an inhibition of stress-induced analgesia (Mogil et al., Neuroscience 75, 1996, pp. 333-337). In this context, also an anxiolytic activity of nociceptin could be detected (Jenck et al., Proc. Natl. Acad. See USA 94, 1997, 14854-14858).
  • Nociceptin has an antinocieptive effect in various models of pain, for example in the mouse tail-tailing test (King et al., Neurosci. Lett., 223, 1997, 113-116) in particular interesting is that the efficacy of nociceptin increases after axillary spinal nerve axotomy. This is in contrast to the classic opioids whose efficacy diminishes under these conditions (Abdulla and Smith, J. Neurosci., 18, 1998, pp. 9685-9694).
  • the ORL1 receptor is also involved in the regulation of other physiological and pathophysiological processes. These include, but are not limited to, learning and memory formation (Manabe et al., Nature, 394, 1997, pp. 577-581), hearing (Nishi et al., EMBO J., 16, 1997, pp. 1858-1864), and numerous others processes.
  • learning and memory formation Manabe et al., Nature, 394, 1997, pp. 577-581
  • hearing Neishi et al., EMBO J., 16, 1997, pp. 1858-1864
  • numerous others processes include, but are not limited to, learning and memory formation (Manabe et al., Nature, 394, 1997, pp. 577-581), hearing (Nishi et al., EMBO J., 16, 1997, pp. 1858-1864), and numerous others processes.
  • CaIo et al. J.J. Pharmacol., 129, 2000, 1261-1283 gives an overview
  • analgesia stimulation and regulation of food intake, influence on ⁇ -agonists such as morphine, treatment of withdrawal symptoms, reduction of the addictive potential of opioids, anxiolysis, modulation of motor activity, memory disorders, epilepsy; Modulation of neurotransmitter release, in particular of glutamate, serotonin and dopamine, and thus neurodegenerative diseases; Influencing the cardiovascular system, triggering an erection, diuresis, antinatriuresis, electrolyte balance, arterial blood pressure, water retention diseases, intestinal motility (diarrhea), relaxing effects on the respiratory tract, micturition reflex (urinary incontinence). Furthermore, the use of agonists and antagonists as anoretic agents, analgesics (also in co-administration with opioids) or nootropics is discussed.
  • WO 2004043967 discloses spirocyclic cyclohexane derivatives which have a high affinity for the ORL1 receptor but also for the ⁇ -opioid receptor. WO 2004043967 also generically describes a group in which R 3 is alkyl or cycloalkyl. However, no example compounds are disclosed which are part of this subgroup.
  • Solubility is an important property for bioavailability and a critical factor in the efficacy and thus the success of drug development.
  • complex processes are used, such as the production of micro- or nanoparticles (eg Exp. Op. Dug Disc., 2007, 2, 145), but the development of compounds that are more equal and easier to plan is simpler and more predictable Effectiveness have a higher solubility.
  • a disadvantage of the example compounds disclosed in WO 2004043967 is the low solubility of the compounds.
  • the object of the present invention was to provide medicaments which act on the nociceptin / ORL1 receptor system and have a higher solubility than the compounds disclosed in WO 2004043967.
  • R 1 and R 2 are independently H; C 3-6 alkyl in each case saturated or unsaturated, branched or unbranched, monosubstituted or polysubstituted or unsubstituted; C ⁇ .s-cycloalkyl, in each case saturated or unsaturated, monosubstituted or polysubstituted or unsubstituted; Aryl, unsubstituted or monosubstituted or polysubstituted; or C 3-6 alkyl-bonded aryl, 03.3- cycloalkyl or heteroaryl, in each case monosubstituted or polysubstituted or unsubstituted;
  • R 1 and R 2 together represent CH 2 CH 2 OCH 2 CH 2 ,
  • .g-alkyl in each case saturated or unsaturated, branched or unbranched, monosubstituted or polysubstituted or unsubstituted;
  • C 3- S -cycloalkyl in each case saturated or unsaturated, monosubstituted or polysubstituted or unsubstituted;
  • R 6 for H; F, Cl, NO 2 , CF 3 , OR 13 , SR 13 , SO 2 R 13 , SO 2 OR 13 , CN, COOR 13 , NR 14 R 15 ;
  • _5-alkyl saturated or unsaturated, branched or unbranched, unsubstituted or monosubstituted or polysubstituted; C3 _8 cycloalkyl, saturated or unsaturated, unsubstituted or mono- or polysubstituted; Aryl or heteroaryl, unsubstituted or monosubstituted or polysubstituted; or about C ⁇
  • _5-alkyl can be replaced;
  • R 14 and R 1 independently of one another H; C ⁇ .g-alkyl, in each case saturated or unsaturated, branched or unbranched, unsubstituted or monosubstituted or polysubstituted; or C3.
  • g-cycloalkyl in each case saturated or unsaturated, unsubstituted or monosubstituted or polysubstituted; Aryl or heteroaryl, unsubstituted or monosubstituted or polysubstituted; or aryl, C 3-8 -cycloalkyl or heteroaryl bonded via C 1-3 -alkyl, unsubstituted or monosubstituted or polysubstituted;
  • R 14 and R 15 together are CH 2 CH 2 OCH 2 CH 2 ,
  • R 16 is H; C 1-10 -alkyl saturated or unsaturated, branched or unbranched, unsubstituted or monosubstituted or polysubstituted;
  • X is O, S, SO, SO 2 or NR 1 7 ;
  • R 1 7 for H; C
  • R 12 is H; C
  • _5-alkyl in each case saturated or unsaturated, branched or unbranched, mono- or polysubstituted or unsubstituted; C 3-8 -cycloalkyl, in each case saturated or unsaturated, monosubstituted or polysubstituted or unsubstituted; Aryl or heteroaryl, in each case monosubstituted or polysubstituted or unsubstituted; or C 3-8 alkyl bonded aryl, C 3-8 cycloalkyl or heteroaryl, in each case monosubstituted or polysubstituted or unsubstituted; OR 13 ; NR 14 R 15 means;
  • R 7 , R 8 , R ⁇ and R 1 ⁇ When summarizing various radicals, for example R 7 , R 8 , R ⁇ and R 1 ⁇ and the summary of radicals on their substituents, such as.
  • OR 13 , SR 13 , SO 2 R 13 or COOR 13 a substituent, for example R 13 , for two or more radicals, such as R ⁇ , R 8 , R ⁇ and R 1 ⁇ 1 assume different meanings within a substance.
  • the compounds of the invention show good binding to the 0RL1 receptor but also to other opioid receptors.
  • _3-alkyl C ⁇
  • Ci.ß alkyl includes for the purposes of this invention acyclic saturated or unsaturated hydrocarbon radicals, which branched or straight chain and unsubstituted or mono- or poly-substituted can be with 1, 2, 3, 4, 5, 6, 7 or 8 C atoms or with 1, 2, 3, 4 or 5 C atoms or 1, 2 or 3 C atoms, ie C - j ⁇ alkanyles, C2_8-alkenyls and C 2 _8-alkynyls or C ⁇
  • Alkenyls have at least one CC double bond and alkynyls at least one CC triple bond.
  • cycloalkyl or "C 3-8 cycloalkyl” for the purposes of this invention means cyclic hydrocarbons having 3, 4, 5, 6, 7 or 8 carbon atoms wherein the hydrocarbons are saturated or unsaturated (but not aromatic), unsubstituted or mono- or can be substituted several times.
  • C 3-3 cycloalkyl is selected from the group consisting of cyclopropyl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl, cyclooctyl, cyclopentenyl, cyclohexenyl, cycloheptenyl and cyclooctenyl.
  • Particularly preferred for the purposes of this invention are cyclobutyl, cyclopentyl and cyclohexyl.
  • (CH 2 ) 3 -6 is -CH 2 -CH 2 -CH 2 -, -CH 2 -CH 2 -CH 2 -CH 2 -, -CH 2 -CH 2 -CH 2 - CH 2 -CH 2 - and CH 2 -CH 2 -CH 2 -CH 2 -CH 2 - to understand.
  • aryl in the context of this invention means carbocyclic ring systems having at least one aromatic ring but without heteroatoms in only one of the rings, i.a. Phenyle, naphthyls and phenanthrenyls, fluoranthenyls, fluorenyls, indanyls and tetralinyls.
  • the aryl radicals can also be condensed with further saturated, (partially) unsaturated or aromatic ring systems.
  • Each aryl radical may be unsubstituted or monosubstituted or polysubstituted, wherein the aryl substituents may be the same or different and may be in any desired and possible position of the aryl. Particularly advantageous are phenyl or naphthyl radicals.
  • heteroaryl represents a 5-, 6- or 7-membered cyclic aromatic radical containing at least 1, optionally also 2, 3, 4 or 5 heteroatoms, wherein the heteroatoms are the same or different and the heterocycle is unsubstituted or may be monosubstituted or polysubstituted; in the case of substitution on the heterocycle, the substituents may be the same or different and may be in any and possible position of the heteroaryl.
  • the Heterocycle may also be part of a bi- or polycyclic system. Preferred heteroatoms are nitrogen, oxygen and sulfur.
  • the heteroaryl radical is selected from the group consisting of pyrrolyl, indolyl, furyl (furanyl), benzofuranyl, thienyl (thiophenyl), benzothienyl, benzothiadiazolyl, benzothiazolyl, benzotriazolyl, benzodioxolanyl, benzodioxanyl, phthalazinyl, pyrazolyl, imidazolyl, Thiazolyl, oxazolyl, isoxazoyl, pyridinyl, pyridazinyl, pyrimidinyl, pyrazinyl, pyranyl, indazolyl, purinyl, indolizinyl, quinolinyl, isoquinolinyl, quinazolinyl, carbazolyl, phenazinyl, phenothiazinyl or oxadiazolyl, wherein the bond to the compounds of general structure
  • alkyl means “C 1-5 alkyl” unless “alkyl” is specified.
  • alkyl and “cycloalkyl” is meant by the term “substituted” in the context of this invention, the substitution of one or more hydrogen radicals by F, Cl, Br, I 1 -CN, NH 2 , NH-alkyl, NH-aryl , NH-heteroaryl, NH-cycloalkyl, NH-alkyl-aryl, NH-alkyl-heteroaryl, NH-alkyl-OH, N (alkyl) 2 , N (alkyl-aryl) 2 , N (alkyl-heteroaryl) 2 , N (Cycloalkyl) 2 , N (alkyl-OH) 2 , NO 2 , SH, S-alkyl, S-aryl, S-heteroaryl, S-alkyl-aryl, S-alkyl-heteroaryl, S-cycloalkyl, S-alkyl- OH, S-alkyl-SH
  • alkyl or cycloalkyl being substituted by F, Cl 1 Br, I 1 CN 1 CH 3 , C 2 H 5 , NH 2 , NO 2 , SH, CF 3 OH, OCH 3 , cyclopentyl, Cyclohexyl, OC 2 H 5 or N (CH 3 ) 2 , preferably F, Cl, Br, I 1 CN, CH 3 , C 2 H 5 , NH 2 , NO 2 , SH 1 CF 3 _OH, OCH 3 , OC 2 H 5 or N (CH 3 ) 2 . It is very particularly preferred if alkyl or cycloalkyl is substituted by OH, OCH 3 or OC 2 H 5 .
  • aryl or “heteroaryl” is understood as meaning “monosubstituted or polysubstituted” the substitution of one or more, for example two, three, four or five times, substitution of one or more hydrogen atoms of the ring system by F , Cl, Br, I 1 CN, NH 2 , NH-alkyl, NH-aryl, NH-heteroaryl, NH-alkyl-aryl, NH-alkyl-heteroaryl, NH-cycloalkyl, NH-alkyl-OH, N (alkyl) 2 , N (alkyl-aryl) 2 , N (alkyl-heteroaryl) 2 , N (cycloalkyl) 2 , N (alkyl-OH) 2 , NO 2 , SH, S-alkyl, S-cycloalkyl, S-aryl, S Heteroaryl, S-alkyl-aryl, S-alkyl
  • salt means any form of the active ingredient according to the invention in which it assumes an ionic form or is charged and is coupled with a counterion (a cation or anion) or is in solution.
  • This also includes complexes of the active ingredient with other molecules and ions, in particular complexes that have ionic interactions are complexed.
  • they include (and this is also a preferred embodiment of this invention) physiologically acceptable salts, especially physiologically acceptable salts with cations or bases and physiologically acceptable salts with anions or acids or else a salt formed with a physiologically acceptable acid or a physiologically acceptable cation ,
  • physiologically acceptable salt with anions or acids is understood as meaning salts of at least one of the compounds according to the invention-usually, for example, nitrogen-protonated-as a cation having at least one anion which is physiologically-in particular when used in humans and / or Mammal - are compatible.
  • a physiologically acceptable acid namely salts of the respective active ingredient with inorganic or organic acids, which are physiologically compatible - in particular when used in humans and / or mammals.
  • physiologically acceptable salts of certain acids are salts of: hydrochloric, hydrobromic, sulfuric, methanesulfonic, formic, acetic, oxalic, succinic, malic, tartaric, mandelic, fumaric, lactic, citric, glutamic, saccharic,
  • Particularly preferred is the hydrochloride salt, citrate and hemicitrate.
  • salt formed with a physiologically acceptable acid means salts of the respective active ingredient with inorganic or organic acids which are physiologically compatible, in particular when used in humans and / or mammals.
  • Particularly preferred is the hydrochloride and the citrate.
  • physiologically compatible acids are: hydrochloric acid, hydrobromic acid, sulfuric acid, methanesulfonic acid, formic acid, acetic acid, oxalic acid, succinic acid, tartaric acid, mandelic acid, fumaric acid, lactic acid, citric acid, glutamic acid, saccharic acid, Monomethylsebacic acid, 5-oxoproline, hexane-1-sulfonic acid, nicotinic acid, 2-, 3- or 4-aminobenzoic acid, 2,4,6-trimethylbenzoic acid, ⁇ -lipoic acid, acetylglycine, acetylsalicylic acid, hippuric acid and / or aspartic acid.
  • physiologically compatible salt with cations or bases refers to salts of at least one of the compounds according to the invention-usually a (deprotonated) acid-as an anion having at least one, preferably inorganic, cation which is physiologically-in particular when used in humans and / or mammalian.
  • Particularly preferred are the salts of the alkali and alkaline earth metals but also ammonium salts, but especially (mono-) or (di) sodium, (mono-) or (di) potassium, magnesium or calcium salts.
  • the term salt formed with a physiologically compatible cation means salts of at least one of the respective compounds as anion with at least one inorganic cation which is physiologically acceptable, in particular when used in humans and / or mammals.
  • Particularly preferred are the salts of the alkali and alkaline earth metals but also ammonium salts, but especially (mono-) or (di) sodium, (mono-) or (di) potassium, magnesium or calcium salts.
  • R 1 and R 2 are independently H; C
  • _5-alkyl in each case saturated or unsaturated, branched or unbranched, monosubstituted or polysubstituted or unsubstituted; C3_ 8 cycloalkyl, in each case saturated or unsaturated, mono- or polysubstituted or unsubstituted; Aryl, unsubstituted or monosubstituted or polysubstituted; or about C
  • R 1 and R 2 together represent CH 2 CH 2 OCH 2 CH 2 , CH 2 CH 2 NR 1 1 CH 2 CH 2 or (CH 2 ) 3 .
  • _3-alkyl in each case saturated or unsaturated, branched or unbranched, monosubstituted or polysubstituted or unsubstituted;
  • C 3-3 -cycloalkyl in each case saturated or unsaturated, monosubstituted or polysubstituted or unsubstituted;
  • R 6 for H; F, Cl, NO 2 , CF 3 , OR 13 , SR 13 , SO 2 R 13 , SO 2 OR 13 , CN, COOR 13 , NR 14 R 1 J5; c
  • R 13 is H; C «
  • _5-alkyl in each case saturated or unsaturated, branched or unbranched, unsubstituted or monosubstituted or polysubstituted; C ⁇ .s-cycloalkyl, in each case saturated or unsaturated, unsubstituted or monosubstituted or polysubstituted; Aryl or heteroaryl, unsubstituted or monosubstituted or polysubstituted; or C-j-alkyl aryl bound .SS, Cß.ß-cycloalkyl or heteroaryl, unsubstituted or singly or multiply substituted;
  • R 14 and R 15 are independently H; C 1-10 -alkyl, in each case saturated or unsaturated, branched or unbranched, unsubstituted or monosubstituted or polysubstituted; or C ⁇ .g-cycloalkyl, in each case saturated or unsaturated, unsubstituted or monosubstituted or polysubstituted; Aryl or heteroaryl, unsubstituted or monosubstituted or polysubstituted; or C-j-alkyl aryl bound .SS, Cß.g- cycloalkyl or heteroaryl, unsubstituted or mono- or polysubstituted alkyl;
  • R 14 and R 15 together form CH 2 CH 2 OCH 2 CH 2 , CH 2 CH 2 NR 16 CH 2 CH 2 or (CH 2 ) 3 _6,
  • R 16 is H; C j _5-alkyl saturated or unsaturated, branched or unbranched, unsubstituted or singly or multiply substituted;
  • X is O, S, SO, SO 2 or NR 17 ;
  • R 17 is H; C ⁇
  • alkyl substituted or cycloalkyl substituted is alkyl or cycloalkyl substituted with F, Cl, Br, I 1 CN, CH 3 , C 2 H 5 , NH 2 , NO 2 , SH, CF 3 OH, OCH 3 , cyclopentyl, Cyclohexyl, OC 2 H 5 or N (CH 3 ) 2 and
  • the Razemats in the form of the Razemats; the enantiomers, diastereomers, mixtures of the enantiomers or diastereomers, or a single enantiomer or diastereomer; the bases and / or salts of physiologically acceptable acids or cations.
  • R 1 and R 2 are independently H, C-
  • R 1 and R 2 independently of one another are H 1 methyl, ethyl, n-propyl, or together are -CH 2 CH 2 CH 2 - or -CH 2 CH 2 CH 2 CH 2 -, wherein preferably only one of the radicals R 1 and R 2 is H.
  • R 1 and R 2 independently of one another are H 1 CH 3 or C 2 H 5 , where not both R 1 and R 2 are H, or R 1 and R 2 form a ring and stand for -CH 2 CH 2 CH 2 - or - CH 2 CH 2 CH 2 CH 2 -.
  • R 1 and R 2 are H or CH 3 , wherein R 1 and R 2 are not simultaneously CH 3 , in particular CH 3 .
  • R 3 is ethyl, n-propyl, 2-propyl, allyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, iso-pentyl, neo-pentyl, n-hexyl, methylcyclopentyl , Methylcyclohexyl, cyclopentyl or cyclohexyl, in each case unsubstituted or monosubstituted or polysubstituted by OH, OCH 3 or OC 2 H 5 . especially
  • R 3 is ethyl, n-propyl, 2-propyl, allyl, n-butyl, iso-butyl, sec-butyl, tert-butyl, n-pentyl, iso-pentyl, neo-pentyl, n-hexyl, cyclopentyl or Cyclohexyl, in each case unsubstituted or monosubstituted or polysubstituted with OH, OCH 3 or OC 2 H 5 .
  • R 5 is H, CH 3 , COOH, COOCH 3, CH 2 OPhenyl, where the phenyl radical is F, Cl 1 Br, I 1 CN, CH 3 , C 2 H 5 , NH 2 , NO 2 , SH, CF 3 ] OH, OCH 3 , OC 2 H 5 or N (CH 3 ) 2 may be substituted, or CH 2 OH.
  • radicals R 7 R 8 , R 9 and R 1 ⁇ for H; C 1-5 -alkyl, branched or unbranched, unsubstituted or monosubstituted or polysubstituted; F, Cl, Br, I, OH, OCH 3 , COOH, COOCH 3 , NH 2 , NHCH 3 or N (CH 3 ) 2 or NO 2 , while the remaining radicals are H,
  • R 7 R 8 , R 9 and R 10 are independently H; C 1-5 -alkyl, branched or unbranched, unsubstituted or monosubstituted or polysubstituted; F, Cl, Br, I, OH, OCH 3 , COOH, COOCH 3 , NH 2 , NHCH 3 or N (CH 3 ) 2 or NO 2 while the remaining radicals are H.
  • spirocyclic cyclohexane derivatives wherein R ⁇ R 8, R 9 and R 1 0 are each H, F, OH, Cl or OCH 3 are.
  • Compounds wherein X is O are most preferred.
  • very particular preference is given to compounds of the general formula I 1 X is NR 17 .
  • spirocyclic cyclohexane derivatives in which R 17 COR 1 2 and R 12 H; C-
  • R 12 H Benzyl, phenethyl, phenethenyl; each unsubstituted or substituted with OCH3; CH3, 2,2-dimethylpropyl or cyclopentyl.
  • the substances according to the invention act, for example, on the 0RL1 receptor relevant in connection with various diseases, so that they are suitable as pharmaceutical active substance in a pharmaceutical.
  • Another object of the invention are therefore medicaments containing at least one inventive spirocyclic cyclohexane derivative, and optionally suitable additives and / or auxiliaries and / or optionally other active ingredients.
  • the medicaments according to the invention optionally contain suitable additives and / or adjuvants, such as carrier materials, fillers, solvents, diluents, dyes and / or binders and can be used as liquid dosage forms in the form of injection solutions, drops or juices, be administered as semi-solid dosage forms in the form of granules, tablets, pellets, patches, capsules, patches / spray patches or aerosols.
  • suitable additives and / or adjuvants such as carrier materials, fillers, solvents, diluents, dyes and / or binders and can be used as liquid dosage forms in the form of injection solutions, drops or juices, be administered as semi-solid dosage forms in the form of granules, tablets, pellets, patches, capsules, patches / spray patches or aerosols.
  • suitable additives and / or adjuvants such as carrier materials, fillers, solvents, diluents, dyes and / or binders
  • the amounts to be used depend on whether the drug is administered orally, perorally, parenterally, intravenously, intraperitoneally, intradermally, intramuscularly, intranasally, buccally, rectally or locally, for example on the skin, mucous membranes or in the mouth the eyes, to be applied.
  • preparations in the form of tablets, dragees, capsules, granules, drops, juices and syrups are suitable, for parenteral, topical and inhalative administration solutions, suspensions, readily reconstitutable dry preparations and sprays.
  • Spirocyclic cyclohexane derivatives according to the invention in a depot, in dissolved form or in a plaster, optionally with the addition of skin penetration-promoting agents, are suitable percutaneous administration preparations. Orally or percutaneously applicable preparation forms can release the spirocyclic cyclohexane derivatives according to the invention with a delay.
  • the spirocyclic cyclohexane derivatives of the invention can also be used in parenteral long-term depot forms such. As implants or implanted pumps are applied. In principle, other active compounds known to the person skilled in the art may be added to the medicaments according to the invention.
  • the amount of drug to be administered to the patient varies depending on the weight of the patient, the mode of administration, the indication and the severity of the disease. Usually, 0.00005 to 50 mg / kg, preferably 0.001 to 0.5 mg / kg of at least one spirocyclic cyclohexane derivative according to the invention are applied.
  • a contained spirocyclic cyclohexane derivative according to the invention is present as a pure diastereomer and / or enantiomer, as a racemate or as a non-equimolar or equimolar mixture of the diastereomers and / or enantiomers.
  • spirocyclic cyclohexane derivatives of the present invention may be used for the manufacture of a medicament for the treatment of pain, especially acute, neuropathic or chronic pain.
  • Another object of the invention is therefore the use of a spirocyclic cyclohexane derivative of the invention for the manufacture of a medicament for the treatment of pain, in particular of acute, visceral, neuropathic or chronic pain.
  • Another object of the invention is the use of a spirocyclic cyclohexane derivative of the invention for the manufacture of a medicament for the treatment of anxiety, stress and stress related syndromes, depression, epilepsy, Alzheimer's disease, senile dementia, general cognitive dysfunction, learning and memory disorders.
  • Disorders (as a nootropic agent), withdrawal symptoms, alcohol and / or drug and / or drug abuse and / or dependence, sexual dysfunctions, cardiovascular diseases, hypotension, hypertension, tinitus, pruritus,
  • Migraine deafness, poor intestinal motility, impaired food intake, anorexia, obesity, locomotor disorders, diarrhea, cachexia, urinary incontinence or as muscle relaxant, anticonvulsant or anesthetic or for coadministration in treatment with an opioid analgesic or anesthetic, for diuresis or antinatriuresis, anxiolysis, modulation of locomotor activity, modulation of neurotransmitter release and treatment of associated neurodegenerative diseases, treatment of withdrawal symptoms and / or reduction of addictive potential opioids.
  • a used spirocyclic cyclohexane derivative is present as a pure diastereomer and / or enantiomer, as a racemate or as a non-equimolar or equimolar mixture of the diastereomers and / or enantiomers.
  • Another object of the invention is a method for the treatment, in particular in one of the aforementioned indications, of a non-human mammal or human, which or a treatment of pain, especially chronic pain, requires, by administering a therapeutically significant dose of a spirocyclic cyclohexane derivative of the invention , or a medicament according to the invention.
  • Another object of the invention is a process for preparing the spirocyclic cyclohexane derivatives of the invention as set forth in the following description and examples.
  • a process for preparing a spirocyclic cyclohexane derivative according to the invention is particularly suitable wherein a cyclohexanone derivative of the general formula E is reacted with an indole derivative of the general formula F or H.
  • At least one reagent from the group of carboxylic acids, phosphoric acids or sulfonic acids or their respective anhydrides, carboxylic acid trialkylsilyl esters, acidic salts, mineral acids or Lewis acids selected from the group consisting of boron trifluoride, indium (III) chloride, titanium tetrachloride, aluminum (III) chloride, or with the addition of at least one transition metal salt, preferably with the addition of at least one transition metal triflate (transition metal trifluoromethanesulfonate), more preferably with the addition of at least one transition metal trifluoromethanesulfonate selected from the group consisting of scandium (III) trifluoromethanesulfonate, ytterbium (III) trifluoromethanesulfonate and indium (III) trifluoromethanesulfonate, optionally with the addition of Celite, with solid-phase-bound reactants or reagents, at elevated or reduced temperature
  • pyridinium para-toluenesulfonate phosphorus pentoxide in the presence of Celite, boron trifluoride etherate, trifluoroacetic acid, orthotitanic acid tetraisopropyl ester together with trifluoroacetic acid, Trifluoromethanesulfonklaretrimethylsilylester, trifluoromethanesulfonic acid, methanesulfonic acid, trifluoroacetic acid, acetic acid, phosphoric acid, polyphosphoric acid, polyphosphate ester, p-toluenesulfonic acid, hydrochloric acid HCl gas, sulfuric acid together with acetate buffer, tin tetrachloride used.
  • Type I secondary amines can be acylated, sulfonylated or carbamoylated by methods known to those skilled in the art to L / M / N type compounds. These reactions are preferably carried out at elevated temperature, particularly preferably under microwave irradiation.
  • Such a method known to the person skilled in the art can be the reaction with an anhydride or an acid chloride with the addition of a base, for example triethylamine.
  • X is selected from the group alkyl, alkyl / alkylidene / aryl or alkyl (saturated / unsaturated) substituted alkylidene
  • Amino acetals Cb having at most one substituent on the nitrogen atom can be prepared by methods known to the person skilled in the art, e.g. be converted by reductive amination, into corresponding amino-acetals Ca with one or two further substituents on the nitrogen.
  • Aminoacetals Cb having at most one substituent on the nitrogen atom can be obtained by addition of carbon nucleophiles to imines Q, preferably organometallic compounds in inert solvents, particularly preferably with Grignard reagents or organolithium compounds, preferably in ethers, preferably at temperatures of -100 to room temperature.
  • Aminoacetals C having two substituents on the nitrogen atom can also be obtained by processes known to those skilled in the art by addition of carbon nucleophiles to salts of enamines Qa, preferably with organometallic compounds in inert solvents.
  • the production of imines is known from the literature.
  • Acetals C can also be obtained by substitution of suitable leaving groups Z in structures of formula B.
  • Suitable leaving groups are preferably cyano groups; 1, 2,3-triazol-1-yl groups.
  • Other suitable leaving groups are 1 H-benzo [d] [1, 2,3] triazol-1-yl groups and pyrazol-1-yl groups (Kathtzky et al., Synthesis 1989, 66-69).
  • a particularly preferred route to compounds of structure C is the reaction of aminonitriles B with corresponding organometallic compounds, preferably Grignard compounds, preferably in ethers, preferably at room temperature.
  • organometallic compounds preferably Grignard compounds, preferably in ethers, preferably at room temperature.
  • the organometallic compounds are either commercially available or can be prepared by known methods.
  • Another particularly preferred route to compounds of structure C is the reaction of aminotriazoles B with corresponding organometallic compounds, preferably Grignard compounds, preferably in ethers, preferably at room temperature.
  • organometallic compounds preferably Grignard compounds, preferably in ethers, preferably at room temperature.
  • the organometallic compounds are either commercially available or can be prepared by literature methods.
  • Structures of formula B can be prepared by reaction of ketones A with amines and acidic reactants ZH. Suitable reactants ZH are z. As hydrogen cyanide, 1, 2,3-triazole, benzotriazole or pyrazole.
  • a particularly preferred route to compounds of structure B is the reaction of ketones with metal cyanides and the corresponding amine in the presence of acid, preferably in an alcohol, at temperatures of - 40 to 60 0 C 1, preferably at room temperature with alkali metal cyanides in methanol.
  • Another particularly preferred route to compounds of structure B is the reaction of ketones with 1,2,3-triazole and the corresponding amine under dehydrating conditions, preferably using a water trap at elevated temperature in an inert solvent or using molecular sieve or a other desiccant.
  • B analogous structures with benzotriazole or pyrazole instead of triazole groups can be introduced.
  • ether means diethyl ether, "EE” ethyl acetate and “DCM” dichloromethane.
  • equivalents means molar equivalents, "mp” melting point or melting range, “decomp.” Decomposition, "RT” room temperature, “abs.” absolute (anhydrous),, “rac.” racemic, “conc.” concentrated, “min” minutes, “h” hours, “d” days, “vol.%” volume percent, “m%” mass percent and “M” is a concentration in mol / l.
  • the stationary phase used for the column chromatography was silica gel 60 (0.040-0.063 mm) from E. Merck, Darmstadt.
  • 1,4-dione monoethylene ketal (30.0 g, 0.192 mol) and potassium cyanide (30.0 g, 0.46 mol).
  • the mixture was stirred at room temperature for 72 h and then extracted with ether (4 x 100 mL) after the addition of water (80 mL).
  • D-1 can also be produced specifically from Erthylmagnesiumbromid and B-1.
  • Phase 2 x with Et 2 Ü (100 ml) extracted.
  • the united org. Phases were washed with water (50 ml) and NaCl solution (50 ml), dried over Na 2 SO 4 , filtered and the solvent i. Vak. away.
  • the residue was dissolved in 2-butanone (200 ml) was added at 0 0 C with Me 3 SiCl (10 mL). The reaction solution was stirred under atmospheric humidity for 5 h and the precipitated solid was filtered off with suction.
  • decane-8-carbonitrile B-1 (10.5 g, 50 mmol) was initially charged in THF (150 mL) under ice-cooling and argon. Within 15 minutes, 2M butylmagnesium chloride in THF (62.5 ml, 125 mmol) was added dropwise and stirred for 16 h at room temperature.
  • the reaction was added under ice-cooling with 20% ammonium chloride solution (37 ml) and water (50 ml) and extracted with ether (3 ⁇ 50 ml).
  • the org. Phase was washed with water (1 x 50 ml) and saturated sodium chloride solution (1 x 50 ml), the organic phase was dried with Na 2 SO 4 and concentrated i. Vak. concentrated.
  • the reaction mixture was extracted with diethyl ether (4 x 100 ml). The organic phase was washed with water (100 ml) and saturated NaCl solution (100 ml), dried and concentrated. There remained a yellow oil (44.5 g), which still contained the educt nitrile in addition to the desired butyl compound.
  • the crude product was dissolved in ethyl methyl ketone (275 ml), admixed with CISiMe 3 (32 ml, 0.245 mol) under ice-cooling and stirred in an open flask at room temperature.
  • the hydrochloride D-2 was separated by repeated filtration at intervals of 2 h. After a Reaction time of 6-8 h, the hydrochloride D-2 could be isolated in a yield of 82% (41, 8 g) as a white solid.
  • Variant 2 4-butyl-4-dimethylamino-cyclohexanone (E-2)
  • the hydrochloride D-2 (41.8 g, 0.15 mmol) was dissolved in water (78 ml) and stirred with ice cooling with 37 percent strength. Hydrochloric acid (100 ml, 1, 2 mol) was added. The clear reaction mixture was stirred for 7 days at room temperature. After completion of the hydrolysis, the reaction mixture was extracted with diethyl ether (2 x 70 ml). The organic extracts were discarded. The aqueous phase was made alkaline with 5N sodium hydroxide solution under ice-cooling (about 250 ml) and stirred vigorously. The solution was extracted with diethyl ether (3 x 100 ml). The combined organic extracts were washed with water (2 x 70 ml), dried and concentrated. The ketone E-2 was recovered as a light brown oil in 96% yield (28.4 g). The yield of ketone E-2 relative to the ketal used in the first step was 75%.
  • the organic phase was distilled under normal pressure.
  • Block E -4
  • 3-Methoxypropan-1-ol (47.1 g, 50 ml, 0.523 mol) was dissolved in pyridine (41.3 g, 42.6 ml, 0.523 mol), cooled to 10 0 C and at 10-30 0 C with vigorous stirring dropwise with thionyl chloride (93.3 g, 56.9 ml, 0.784 mol) were added. A solid precipitate was precipitated, the mixture was then stirred at 65 ° C for 3 h.
  • the desiccant was filtered off and the organic phase washed with « 2 CO 3 solution until alkaline reaction.
  • the organic phase was separated, washed with water and dried over K 2 CO 3 , filtered and distilled at normal pressure.
  • the amine C-4 (8.11 g, 31.5 mmol) was dissolved in water (12 ml), with ice cooling with conc. HCl (19.5 ml) and stirred for 3 d at room temperature.
  • the reaction mixture was washed with ether (2 x 75 ml).
  • the solution was then basified with 5N NaOH and extracted with dichloromethane (3 x 75 ml).
  • the combined organic phases were washed with water (75 ml), dried over Na 2 SO 4 , filtered and the solvent i. Vak. away.
  • the ketal C-6 (0.68 g, 2.68 mmol) was added with 6N hydrochloric acid (5 ml) and stirred at room temperature overnight. After the hydrolysis had ended, the reaction mixture was extracted with ether (2 ⁇ 20 ml), the aqueous solution was made alkaline with 5N sodium hydroxide solution under ice-cooling, extracted with dichloromethane (3 ⁇ 10 ml), the organic phase was dried over sodium sulfate and concentrated by evaporation. Vak. concentrated.
  • reaction mixture was cautiously mixed with saturated ammonium chloride solution (60 ml) while cooling with ice, the pH was adjusted to 10 with sodium hydroxide solution and extracted with diethyl ether (3 ⁇ 50 ml). The combined organic phases were dried with sodium sulfate and i. Vak. concentrated. The crude product was reacted further without purification.
  • reaction solution was i. Vak. concentrated and the residue dissolved in anhydrous tetrahydrofuran.
  • the reaction mixture was warmed slowly to room temperature and stirred overnight.
  • reaction mixture was added with ice-cooling with water (40 ml) and extracted with diethyl ether (3 x 50 ml).
  • the combined organic phases were dried with sodium sulfate, i. Vak. concentrated and the residue by means of
  • the reaction mixture was stirred for 2 h at room temperature and then added dropwise with ice-water cooling to 20% ammonium chloride solution (120 ml).
  • the organic phase was separated and the aqueous phase extracted with ethyl acetate (3 x 100 ml).
  • the combined organic phases were washed with 2N sodium hydroxide solution (100 ml) and water (100 ml), dried with sodium sulfate and concentrated i. Vak. concentrated.
  • the crude product (7.67 g) was purified by flash chromatography (400 g, 20 ⁇ 7.5 cm) with ethyl acetate / cyclohexane (1: 2).
  • reaction solution was transferred to a sealable graduated cylinder and the crude product further used in.
  • reaction mixture was stirred for 2 h at room temperature and then cooled to 0 0 C and added dropwise to a 20% ammonium chloride solution (50 ml), the aqueous phase with diethyl ether (3 x 40 ml) extracted, the combined organic phases were washed with 2 N sodium hydroxide solution (70 ml) and water (70 ml), dried with sodium sulfate and i. Vak. concentrated.
  • reaction solution was subsequently refluxed for 30 min, cooled to RT and treated with a solution of 8-dimethylamino-1,4-dioxa-spiro [4.5] decane-8-carbonitrile B-1 (10.5 g, 50 mmol) in abs. THF (100 mL) was added dropwise. The reaction solution boiled and a white solid precipitated. It was refluxed for 6 h and then stirred at RT overnight. To work up the reaction mixture was added under ice cooling 20% NH 4 Cl solution (200 mL) and extracted with ether (3 x 100 mL). The organic phase was dried over Na 2 SO 4 and i. Vak. concentrated. The remaining residue was purified by flash chromatography with EE / EtOH (20: 1).
  • the aqueous phase was alkaline with 5N NaOH under ice bath cooling and extracted with dichloromethane (3 x 50 ml). The organic phase was dried over Na 2 SO 4 and i. Vak. concentrated to dryness.
  • the batch was admixed with 1 N NaOH and extracted with CH 2 Cl 2 (3 ⁇ 15 ml).
  • the org. Phase was dried over Na 2 SO 4 and i. Vak. concentrated.
  • Of the Residue was purified by flash chromatography with CHCl 3 Z MeOH (9: 1) followed by recrystallization from ethanol.
  • Example AA-5 ⁇ '-fluoro-1 ', S'-dihydro-N, N-dimethyl-butyl-spiro-cyclohexane-i.rtS ⁇ ) pyrano [3,4-b] indole] -4-amine, 2-hydroxy 1,2,3-propanetricarboxylate (2: 1) (one of 2 possible diastereomers)
  • the NMR spectra of the free base were evaluated because the spectra of the citrate were poorly resolved.
  • Example AA- ⁇ ⁇ '-FluoM'.S'-dihydro-N, N-dimethyM-butyl-spiro-cyclohexane-i, 1 '(3 1 H) -pyrano [3,4-b] indole] -4-amine, 2 -hydroxy-1,2,3-propanetricarboxylate (1: 1) (one of 2 possible diastereomers)
  • Example AA-6 was prepared analogously to Example AA-5. In citrate precipitation, however, citrate was isolated instead of hemicitrate.
  • Example AA-7 ⁇ '-hydroxy ⁇ ', S'-dihydro-N, N-dimethyl-A-butyl-spiro-cyclohexane-I.IXS ⁇ ) -pyrano [3,4-b] indole] -4-amine, 2,2 , 2-trifluoroacetate (1: 1) (one of 2 possible diastereomers)
  • the aqueous phase was extracted with dichloromethane (2 x 20 ml). The organic phase was dried over Na 2 SO 4 and i. Vak. concentrated. The just obtained cyclization product (100 mg, 0.273 mmol) was dissolved in hot ethanol (5 ml). The citric acid (52 mg, 0.273 mmol) dissolved in hot ethanol was added. The reaction was cooled to room temperature, whereupon a white precipitate was precipitated. The precipitate AA-7 was i. Vak. dried.
  • Trifluoroacetic acid was probably introduced by mistake, so that not the desired citrate but a trifluoroacetic acid salt was obtained.
  • Example AA-8 e'-hydroxy- ⁇ , ⁇ '-dihydro-N, N-dimethyl-butyl-spiro-cyclohexane-ii (a'H) -pyrano [3,4-b] indole] -4-amine, 2- Hydroxy-1,2,3-propanetricarboxylate (2: 3) (One of 2 possible diastereomers
  • the aqueous phase was extracted with 1, 2-dichloroethane (2 x 70 ml).
  • the organic phases were combined, washed with water (50 ml), dried and concentrated.
  • the brown oily residue was added with methanol (60 ml), which crystallized.
  • the suspension was stirred for a further 10 minutes.
  • the colorless crystals were filtered off with suction and washed with methanol (60 ml) (1.28 g). This was the pure nonpolar spiroamine.
  • the filtrate was concentrated and the resulting brown solid was re-added with methanol (50 ml) and stirred for 1 h in an ice bath.
  • the nonpolar spiroamine just prepared (92 mg, 0.27 mmol) was dissolved in hot ethanol (5 ml).
  • the citric acid (51 mg, 0.27 mmol) dissolved in hot ethanol was added.
  • the reaction was cooled to room temperature, whereupon a white precipitate was precipitated.
  • the precipitate AA-9 was filtered off and i. Vak. dried.
  • Example AA-10 ⁇ '.S ' ⁇ ', S'-Tetrahydro-N, N-dimethyl-butyl-Z'-methylcarbonyl-spiro-cyclohexane-1,1 '(1'H) -pyrido [3,4-b] indole] -4-amine, 2-hydroxy-1,2,3-propanetricarboxylate (1: 1) (nonpolar diastereomer)
  • Acetyl chloride (0.126 mL, 139 mg, 1.77 mmol) was added under argon in abs.
  • Dichloromethane (5 ml) and treated at room temperature with the free base of the nonpolar spiroamine AA-9 (200 mg, 0.59 mmol), dissolved in dichloromethane (15 ml), within 30 min. After 15 minutes, a precipitate was visible, which had dissolved again at the end of the addition. After a reaction time of 30 min, a precipitate was formed again. It was stirred for a further 21 h at room temperature. For workup, the colorless batch was mixed with water (10 ml) and 1N sodium hydroxide solution (5 ml) and stirred for 1 h. The phases were separated.
  • the less polar amide just prepared (125 mg, 0.327 mmol) was added at 50 0 C in ethanol (5 ml) and treated with an ethanolic solution (3 ml) was added citric acid (70 mg, 0.36 mmol). After a reaction time of 3 h at room temperature, the colorless citrate AA-10 was separated by filtration and washed with ethanol (2 x 3 ml). The less polar amide (118 mg) as a citrate in a yield of 63% with a melting point of 220-222 0 C.
  • Example AA-11 Z'S '' '', S'-Tetrahydro-N, N-dimethyl-butyl-1'-cyclopentylcarbonyl spiro [cyclohexane-1,1 '(1'H) -pyrido [3,4-b] indole] -4-amine, 2-hydroxy-1,2,3-propanetricarboxylate (2: 1) Nonpolar diastereomer
  • the amide was isolated as a colorless hygroscopic solid in 87% yield (222 mg).
  • the amide just obtained (186 mg, 0.427 mmol) was added (8 ml) at 60 0 C in ethanol and treated with an ethanolic solution (3 ml) of citric acid (90 mg, 0.47 mmol). A precipitation started immediately. After a reaction time of 2 h at room temperature, the colorless citrate AA-11 was separated by filtration and washed with ethanol (2 x 3 ml). The less polar amide (183 mg) as a citrate in a yield of 69% with a melting point of 228-230 0 C.
  • 3,3-Dimethylbutyric acid chloride (0.246 mL, 238 mg, 1.77 mmol) was added under argon in abs.
  • Dichloromethane (5 ml) and treated at room temperature with the free base of the nonpolar spiroamine AA-9 (200 mg, 0.59 mmol), dissolved in dichloromethane (15 ml), within 30 min.
  • the yellow reaction solution was treated with water (10 ml) and 1 N sodium hydroxide solution (5 ml) and stirred for 1 h.
  • the phases were separated.
  • the aqueous phase was extracted with dichloromethane (20 ml).
  • the combined organic phases were washed with water (20 ml), dried and concentrated.
  • Example AA-13 2 ', 3 1, 4 1, 9 l -tetrahydro-N, N-dimethyl-4-butyl-l 2 - (3,4-dimethoxybenzylcarbonyl) - spiro [cycIohexan-1,1' (1 ⁇ ) -pyrido [3,4-b] indole] -4-amine, 2-hydroxy-1,2,3-propanetricarboxylate (1: 1) (nonpolar diastereomer)
  • non-polar amide (216 mg, 0.417 mmol) was dissolved at 60 0 C in ethanol (11 ml) and with an ethanolic solution (3 ml) was added citric acid (89 mg, 0.46 mmol). After a reaction time of 5 h at room temperature, the colorless citrate was separated by filtration and washed with ethanol (2 x 3 ml). The non-polar amide was obtained in a yield of 92% (270 mg) was obtained as citrate AA-13 with a melting point of 188-190 0 C.
  • the free base of the nonpolar spiroamine AA-9 (204 mg, 0.6 mmol) was dissolved in abs. Acetonitrile (30 ml) and treated with ethyl isocyanate (0.052 ml, 47 mg, 0.66 mmol). The reaction mixture was heated at reflux for 6 hours. The clear solution was concentrated. The oily residue was taken up in diethyl ether (20 ml) and washed with water (5 ml). After drying and concentration, the non-polar urea was obtained as a colorless solid in a yield of 57% (139 mg) with a melting point of 154-158 ° C.
  • apolar urea (139 mg, 0.4 mmol) just obtained was dissolved in ethanol (10 ml) and treated with an ethanolic solution (5 ml) of citric acid (85 mg, 0.44 mmol). After a reaction time of 20 h at room temperature, the colorless citrate was separated by filtration. Since the product had a greasy consistency, it was washed with diethyl ether (2 x 3 ml). Additional product could not be recovered from the filtrate. The non-polar urea was obtained in a yield of 38% (90 mg) was obtained as citrate AA-14 with a melting point of 215- 231 0 C.
  • the free base of the nonpolar spiro amine AA-9 (200 mg, 0.59 mmol) was added (0.04 ml) was added with water and at 0 0 C in 95 percent strength.
  • Formic acid (0.6 ml, 732 mg, 15.9 mmol). At this temperature was 37 percent.
  • aqueous formaldehyde solution (0.46 ml, 178 mg, 5.9 mmol) was added, stirred for 10 min in an ice bath and the mixture heated to 100 0 C for 1 h. Under ice-cooling, the beige solution was added with water (5 ml) and 1N sodium hydroxide solution (15 ml).
  • non-polar spiro amine 51 mg, 0.144 mmol was added (2 ml) at 60 0 C in ethanol and treated with an ethanolic solution (2 ml) of citric acid (64 mg, 0.316 mmol) was added. After a reaction time of 6 h, the citrate 5/6 was filtered off with suction as a colorless solid, washed with ethanol (2 ⁇ 2 ml) and diethyl ether (2 ⁇ 5 ml). The less polar spiro-amine was obtained as hygroscopic citrate AA-16 in 47% yield (37 mg)
  • Example AA-17 ⁇ '-fluoro '', S'-dihydro-N-ethyl-N-methyl-butyl-spiro-cyclohexane-I, Si-S-pyrano [3,4-b] indole] -4- amine, 2-hydroxy-1,2,3-propanetricarboxylate (1: 1) (one of 2 possible diastereomers)
  • E-7 500 mg, 2 mmol
  • 5-fluorotryptophol F-2 430 mg, 2.4 mmol
  • trifluoromethanesulfonic acid 450 mg, 265 ⁇ L, 3 mmol
  • reaction mixture was admixed with 0.5 N sodium hydroxide solution (10 ml), stirred at room temperature for 2 h, the organic phase was separated off and the aqueous phase was extracted with dichloromethane (2 ⁇ 20 ml). The combined organic phases were dried with sodium sulfate and i. Vak. concentrated.
  • the crude product was purified by flash chromatography (100 g, 20 x 4.0 cm) with cyclohexane / ethyl acetate (9: 1) and 1% triethylamine. Yield: 469 mg (53%), white solid Melting point: 112-121 0 C.
  • Example AA-18 e'-fluoro-A'. ⁇ '-dihydro-N-benzyl-N-methyl-spirotcyclohexane-II-butyl (S, S) -pyrano [3,4-b] indol-4-amine (one of 2 possible diastereomers )
  • reaction mixture was treated with 0.5 N sodium hydroxide solution (10 ml), stirred for 2 h at room temperature, the organic phase separated, the aqueous phase extracted with dichloromethane (2 x 20 ml), the combined organic phases dried with sodium sulfate and i. Vak. concentrated. Subsequently, the crude product was purified by flash chromatography (18 g, 20 ⁇ 2.0 cm) with cyclohexane / ethyl acetate (9: 1) and 1% triethylamine.
  • the organic phase was separated, the aqueous extracted with dichloromethane (3 x 20 ml), the combined organic phases were washed with sodium chloride solution (50 ml), dried with sodium sulfate and concentrated i. Vak. concentrated.
  • the isomer mixture (815 mg) was separated by flash chromatography (100 g, 22 x 4 cm) with ethyl acetate / cyclohexane (1: 3).
  • Example AA-21 The polar diastereomer obtained under Example AA-20 is continued as Example AA-21.
  • the ketone E-4 (275 mg, 1.26 mmol) and tryptophol F-1 (206 mg, 1.26 mmol) were dissolved in abs. Dissolved dichloromethane (10 ml) under argon with methanesulfonic acid (0.13 ml, 2.05 mmol) and stirred for 20 h at room temperature. After addition of 1 N NaOH (10 ml) and CH 2 Cl 2 (20 ml) was stirred for 10 min, the phases were separated, the aqueous phase extracted twice with CH 2 Cl 2 , the combined organic phases washed with water, over Na 2 SO 4 dried and the solution i. Vak. concentrated. The remaining residue was purified by FlasH chromatography with CHCl 3 / MeOH (20: 1).
  • Example AA-23 ⁇ '-FluoM'.S'-dihydro-N, N-dimethyl-A-methoxypropyl-spirotcyclohexane-i.i'tS'H) -pyrano [3,4-b] indole] -4-amine, 2-hydroxy-1,2,3-propanetricarboxylate (1: 1)
  • the ketone E-4 (426 mg, 2 mmol) and tryptamine H-1 (320 mg, 2 mmol) were dissolved in abs. Dissolved methanol (10 ml) and stirred for 20 h at room temperature. Subsequently the solvent was i. Vak. The residue was dissolved in DCE (20 ml), added with trifluoroacetic acid (2 ml) and stirred at room temperature for 5 h.
  • the ketone E-3 (455 mg, 2 mmol) and tryptophol F-1 (326 mg, 2 mmol) were dissolved in abs. Dissolved dichloromethane (10 ml), under argon with methanesulfonic acid (0.14 ml, 2.2 mmol) and stirred for 24 h at room temperature. After addition of 1N NaOH (15 ml) and CH 2 Cl 2 (25 ml) stirring was continued for 10 minutes, then the phases were separated, the aqueous phase extracted twice with CH 2 Cl 2 (10 ml), the combined organic Washed with water (10 ml), dried over Na 2 SO 4 and the solution i. Vak. concentrated. The remaining residue was purified by FlasH chromatography with CHCl 3 / MeOH (20: 1).
  • the ketone E-3 (455 mg, 2 mmol) and tryptamine H-1 (320 mg, 2 mmol) were dissolved in abs. Dissolved methanol (10 ml) and stirred at room temperature for 20 h. Subsequently, the solvent was i. Vak. The residue was dissolved in DCE (20 ml), added with trifluoroacetic acid (2 ml) and stirred at room temperature for 5 h.
  • the ketone E-6 (235 mg, 1.1 mmol) and tryptophol F-1 (180 mg, 1.12 mmol) were dissolved in abs. Dissolved dichloromethane (5 ml) and under argon with methanesulfonic acid (0.1 ml, 1.5 mmol) and stirred for 20 h at room temperature. After addition of 1 N NaOH (5 ml) and CH 2 Cl 2 (10 ml) was stirred for 10 min, the phases were separated, the aqueous phase extracted twice with CH 2 Cl 2 , the combined organic phases washed with water, dried ( Na 2 SO 4 ) and the solution i. Vak. concentrated. The remaining residue was purified by FlasH chromatography with CHCb / MeOH (20: 1).
  • Example AA-29 ⁇ '.S ' ⁇ ', ⁇ '-tetrahydro-N, N-dimethyl-cyclopentyl spiro cyclohexane-i, 1 '( 1 H) -pyrido [3,4-b] indole] -4-amine, 2-hydroxy 1,2,3-propanetricarboxylate (1: 1) (one of 2 possible diastereomers)
  • the ketone E-6 (209 mg, 1.0 mmol) and tryptamine H-1 (160 mg, 1.0 mmol) were dissolved in abs. Dissolved methanol (10 ml) and stirred at room temperature for 20 h. Subsequently, the solvent was i. Vak. The residue was dissolved in dichloroethane (10 ml), added with trifluoroacetic acid (1.0 ml) and stirred at room temperature for 5 d.
  • ketone E-5 (175 mg, 0.78 mmol) and tryptophol F-1 (126 mg, 0.78 mmol) were dissolved in abs.
  • Dichloromethane (5 ml) and dissolved under argon with methanesulfonic acid
  • Example AA-31 ⁇ '-fluoro-'' S'-dihydro-N, N'-dimethyl-cyclohexyl-spiro-cyclohexane-i.i'CS'H) -pyrano [3,4-b] indole] -4-amine; 2-hydroxy-1,2,3-propanetricarboxylate (1: 1) (one of 2 possible diastereomers)
  • the ketone E-5 (175 mg, 0.78 mmol) and tryptamine H-1 (125 mg, 0.78 mmol) were dissolved in abs. Dissolved methanol (8 ml) and stirred at room temperature for 20 h. Subsequently, the solvent was i. Vak. The residue was dissolved in dichloroethane (10 ml), added with trifluoroacetic acid (0.8 ml) and stirred at room temperature for 4 h.
  • Example AA-9 The more polar spiroether (90 mg, 0.26 mmol) prepared in Example AA-9 was dissolved in hot ethanol (5 ml). The citric acid (48 mg, 0.26 mmol) dissolved in hot ethanol was added. The reaction was cooled to room temperature, whereupon a white precipitate was precipitated. The precipitate was filtered off and i. Vak. dried.
  • Example AA-34 ⁇ '-FluoM'.S'-dihydro-N, N-dimethyl-ethyl-spirotcyclohexane-i.rtS ⁇ -pyrano [3,4-b] indole] -4-amine, 2-hydroxy-1 , 2,3-propanetricarboxylate (1: 1) (polarer diastereomer)
  • the ketone E-4 (426 mg, 2 mmol) and tryptamine H-1 (320 mg, 2 mmol) were dissolved in abs. Dissolved methanol (10 ml) and stirred for 20 h at room temperature. Subsequently, the solvent was i. Vak. The residue was dissolved in DCE (20 ml), added with trifluoroacetic acid (2 ml) and stirred at room temperature for 5 h.
  • Example AA-36 ⁇ '-fluoro- ⁇ '-dihydro-N, N-dimethyl-methoxypropyl spiro-cyclohexane-i J '(3 ⁇ ) pyrano [3,4-b] indole] -4-amine, 2-hydroxy-1 , 2,3-propanetricarboxylate (1: 1) (polarer diastereomer)
  • the ketone E-4 (426 mg, 2 mmol) and 5-fluoro-tryptophol F-2 (362 mg, 2 mmol) were dissolved in abs.
  • Ketone E-2 (2.0 g / 10.15 mmol) and tryptophol F-1 (1.63 g / 10.15 mmol) were dissolved under argon in abs.
  • Submitted dichloromethane (70 ml) and then treated with methanesulfonic acid (720 ul / 11.16 mmol).
  • the batch was stirred for 24 h at room temperature.
  • the batch was admixed with 1 N NaOH and extracted with dichloromethane (3 ⁇ 15 ml).
  • the organic phase was dried over Na 2 SO 4 and i. Vak. concentrated.
  • the residue was purified by flash chromatography with CHCb / MeOH (9: 1, 1: 1).
  • the ketone E-3 (455 mg, 2 mmol) and tryptamine H-1 (320 mg, 2 mmol) were dissolved in abs. Dissolved methanol (10 ml) and stirred at room temperature for 20 h. Subsequently, the solvent was i. Vak. removed, the residue dissolved in DCE (20 ml), washed with Trifluoroacetic acid (2 ml) and stirred for 5 h at room temperature.
  • the product was present as hydrochloride.
  • the hydrogen chloride comes from the chloroform used for chromatography.
  • fraction 1 (350 mg, 0.83 mmol) in chloroform (20 ml) was washed with sodium bicarbonate solution, the organic phase was dried with sodium sulfate and concentrated i. Vak. concentrated.
  • Example AA-47 is the citrate of the nonpolar diastereomer (fraction 1) obtained in example AA-38. This citrate was precipitated according to the standard procedure.
  • the nonpolar diastereomer (991 mg, 2.78 mmol) just obtained was dissolved in hot ethanol and dissolved with citric acid (529 mg, 2.78 mmol) in ethanol (5 ml). The precipitate was filtered off with suction and i. Vak. dried.
  • Example AA-48 The more polar diastereomer (900 mg, 2.52 mmol) obtained in Example AA-48 was dissolved in hot ethanol / dioxane (5 ml, 30 ml) (poorly soluble). Then, citric acid (480 mg, 2.52 mmol) was dissolved in hot ethanol (5 ml) and added. The batch was cooled to RT with little precipitation, so ether was added. The precipitate was filtered off with suction and i vac. dried.
  • the ketone E-17 (223 mg, 1.0 mmol) and 5-fluoro-tryptophol (179 mg, 1.0 mmol) were dissolved in abs. Dissolved dichloromethane (10 ml), under argon with methanesulfonic acid (0.1 ml, 1.5 mmol) and stirred at RT for 3 d. After addition of 1N NaOH (10 ml) and CH 2 Cl 2 (20 ml), the mixture was stirred for a further 10 min, the phases were separated, the aqueous phase was extracted twice with CH 2 Cl 2 , the combined organic phases were washed with water, dried ( Na 2 SO 4 ) and i. Vak. concentrated.
  • Tetra hydrofu ran (30 ml) and dissolved at room temperature with the free base of the nonpolar spiroamine prepared under Example AA-9 (300 mg, 0.88 mmol), dissolved in abs. Tetrahydrofuran (15 ml), added within 20 min. This resulted in a strong precipitation.
  • the reaction mixture was diluted with water (10 ml), admixed with 1N sodium hydroxide solution (10 ml) with ice cooling and then stirred for 2 hours. Tetrahydrofuran was removed in vacuo. As a result, a solid precipitated, which was separated by filtration and washed with water (3 ⁇ 10 ml).
  • the crude product (408 mg) was separated by chromatography [Kieselgel 60 (50 g); Ethyl acetate (500 ml)]. The less polar amide was recovered as a colorless solid in 76% yield (314 mg).
  • the non-polar amide just obtained (296 mg, 0.63 mmol) was suspended at 80 ° C. in ethanol (14 ml) and treated with an ethanolic solution (3 ml) of citric acid (133 mg, 0.69 mmol). From the clear solution, a solid precipitated on cooling to room temperature. It was stirred for 16 h at room temperature. The mixture was stored at 5 ° C. for 2 h. The colorless solid was separated by filtration and washed with diethyl ether (3 x 3 ml). The nonpolar citrate AA-51 was thus obtained in a yield of 85% (302 mg) as hemicitrate with a melting point of 154-157 0 C.
  • aqueous buffers were used at various pH's (pH 1, 100mM HCl, pH 2, 10mM HCl, pH 4, 50mM citric acid, titrated with 1 N NaOH; pH 6, 50 mM sodium citrate, titrated with 1 N HCl; pH7, 50 mM Tris.HCl; pH 8, Tris.HCI), which maintained the adjusted pHs at room temperature in the final solution.
  • DMSO metastable supersaturated aqueous solutions with increasing concentration
  • the stock solutions were diluted 1: 100 in aqueous buffer.
  • the solutions were shaken in closed containers for at least 15 hours.
  • 10 ⁇ l of DMSO stock solution were diluted in 990 ⁇ l of aqueous buffer and placed in suitable vessels (eg Eppendorf vessels) so that the concentration was constant at 1% v / v.
  • suitable vessels eg Eppendorf vessels
  • the calibration solutions were prepared by dilution of the stock DMSO in methanol (1: 100). From these dilutions further dilutions were made in methanol (1: 100, 1: 200, 1: 400 and 1: 800). Samples were analyzed by RP-HPLC with UV detection. Regression analysis derived linear calibration equations, generally with correlation coefficients greater than 0.95. Using the calibration equations determined experimentally, the concentrations of the compounds in the buffer solutions were determined. With the described experiment maximum concentrations of 200 ⁇ g / ml substance in buffer could be determined. Higher solubilities could not be quantified.
  • the compounds according to the invention have an extremely high affinity for the 0RL1 or the ⁇ -opioid receptor.
  • the affinity is of the same order of magnitude as the two comparison compounds. However, they have a higher solubility.
  • the cyclohexane derivatives of the general formula I were investigated in a receptor binding assay with 3 H-nociceptin / orphanin FQ with membranes from recombinant CHO-ORL1 cells.
  • This test system was tested according to the method described by Ardati et al. (Mol. Pharmacol., 51, 1997, pp. 816-824).
  • the concentration of 3 H-nociceptin / orphanin FQ was 0.5 nM in these experiments.
  • the binding assays were carried out with 20 ⁇ g membrane protein per 200 ⁇ l batch in 50 mM Hepes, pH 7.4, 10 mM MgCl 2 and 1 mM EDTA.
  • the binding to the ORL1 receptor was carried out using 1 mg WGA-SPA beads (Amersham-Pharmacia, Freiburg), by incubation of the batch at room temperature for one hour and subsequent measurement in the scintillation counter Trilux
  • the incubation buffer used was 50 mmol / l Tris-HCl supplemented with 0.05% by weight of sodium azide and with 0.06% by weight of bovine serum albumin. To determine the unspecific binding an additional 25 .mu.mol / l naloxone was added. Upon completion of the ninety minute incubation period, the Centrifuge microtiter plates for 20 minutes at 1000 g and measure the radioactivity in a ⁇ -counter (Microbeta-Trilux, PerkinElmer Wallac, Freiburg, Germany). The percentage displacement of the radioactive ligand from its binding to the human ⁇ -opiate receptor was determined at a concentration of the test substances of 1 ⁇ mol / l and as a percentage inhibition
  • mice were individually placed in a test cage and the tail base exposed to the focused heat beam of an electric lamp (tail-flick type 50/08/1, bc, Labtec, Dr. Hess). The lamp intensity was adjusted so that the time from switching on the lamp to the sudden winceing of the tail (pain latency) in untreated mice was 3 to 5 seconds. Before the application of the solutions containing the compound of the invention or the respective comparative solutions, the mice were pretested twice within five minutes and the mean of these measurements was calculated as the pretest mean value.
  • the solutions of the compound of general formula I according to the invention and the comparative solutions were then administered intravenously.
  • the pain measurement was carried out in each case 10, 20, 40 and 60 minutes after the intravenous application.
  • the analgesic effect was determined as an increase in pain latency (% of the maximum possible antinociceptive effect) according to the following formula:
  • the time T 0 is the latency before the application
  • the time Ti the latency after the application of the active substance combination
  • the time T 2 the maximum exposure duration (12 seconds).
  • test was carried out in an analogous manner in the rat.

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Abstract

L'invention concerne des dérivés de cyclohexane spirocycliques de formule (I), des procédés pour leur production, des médicaments contenant ces composés, ainsi que l'utilisation de dérivés de cyclohexane spirocycliques pour produire des médicaments. R<SUP>3</SUP> est un groupe alkyle ou cycloalkyle (substitué), ce qui entraîne une augmentation de la solubilité.
PCT/EP2008/001270 2007-02-22 2008-02-19 Dérivés de cyclohexane spirocycliques WO2008101659A1 (fr)

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CA2679166A CA2679166C (fr) 2007-02-22 2008-02-19 Derives de cyclohexane spirocycliques
ES08707767T ES2433205T3 (es) 2007-02-22 2008-02-19 Derivados de ciclohexano espirocíclicos
RU2009135072/04A RU2484092C2 (ru) 2007-02-22 2008-02-19 Спироциклические производные циклогексана
NZ578717A NZ578717A (en) 2007-02-22 2008-02-19 Spirocyclic cyclohexane derivatives
JP2009550239A JP5366832B2 (ja) 2007-02-22 2008-02-19 スピロ環式シクロヘキサン誘導体
KR1020097019744A KR101515795B1 (ko) 2007-02-22 2008-02-19 스피로사이클릭 사이클로헥산 유도체
BRPI0806796-1A BRPI0806796A2 (pt) 2007-02-22 2008-02-19 derivados de ciclohexano espiro cìclico
CN2008800059845A CN101622255B (zh) 2007-02-22 2008-02-19 螺环状的环己烷衍生物
AU2008217276A AU2008217276B2 (en) 2007-02-22 2008-02-19 Spirocyclic cyclohexane derivatives
PL08707767T PL2121689T3 (pl) 2007-02-22 2008-02-19 Spirocykliczne pochodne cykloheksanu
MX2009008781A MX2009008781A (es) 2007-02-22 2008-02-19 Derivados de ciclohexano espirociclicos.
EP08707767.3A EP2121689B1 (fr) 2007-02-22 2008-02-19 Dérivés de cyclohexane spirocycliques
HK10103564.8A HK1136828B (en) 2007-02-22 2008-02-19 Spirocyclic cyclohexane derivatives
IL200497A IL200497A (en) 2007-02-22 2009-08-20 History of Spirocyclic Cyclohexane
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US8993765B2 (en) 2010-12-21 2015-03-31 Albany Molecular Research, Inc. Tetrahydro-azacarboline MCH-1 antagonists, methods of making, and uses thereof
US9073925B2 (en) 2009-07-01 2015-07-07 Albany Molecular Research, Inc. Azinone-substituted azabicycloalkane-indole and azabicycloalkane-pyrrolo-pyridine MCH-1 antagonists, methods of making, and use thereof
US10202345B2 (en) 2014-07-15 2019-02-12 Gruenenthal Gmbh Substituted azaspiro(4.5)decane derivatives
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MX345068B (es) * 2010-08-04 2017-01-16 Gruenenthal Gmbh Forma de dosificacion farmaceutica que comprende 6'-fluoro-(n-metil- o n,n-dimetil-)-4-fenil-4', 9'-dihidro-3'h-espiro[ciclohexan-1,1'-pirano[3,4,b]indol]-4-amina .
ES2653715T3 (es) * 2010-12-08 2018-02-08 Grünenthal GmbH Procedimiento para sintetizar derivados de aminociclohexanona sustituidos
CN102659662A (zh) * 2012-03-28 2012-09-12 华东师范大学 3-r-3-羟基-2-氧化吲哚类化合物的合成方法

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004043967A1 (fr) * 2002-11-11 2004-05-27 Grünenthal GmbH Derives de cyclohexane spirocycliques
WO2006108565A1 (fr) * 2005-04-11 2006-10-19 Grünenthal GmbH Derives de cyclohexane spirocycliques permettant de traiter une dependance a une substance
WO2008009415A2 (fr) * 2006-07-18 2008-01-24 Grünenthal GmbH Dérivés hétéroaryliques substitués

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1055203A (en) * 1964-09-16 1967-01-18 Ici Ltd -ß-carboline derivatives, a process for their manufacture, and compositions containing them
US4291039A (en) * 1980-08-08 1981-09-22 Miles Laboratories, Inc. Tetrahydro β-carbolines having anti-hypertensive activity
DE3309596A1 (de) * 1982-08-05 1984-04-05 Basf Ag, 6700 Ludwigshafen 2-substituierte 1-(3'-aminoalkyl)-1,2,3,4-tetrahydro-ss-carboline, ihre herstellung und verwendung als arzneimittel
US5328905A (en) * 1987-07-20 1994-07-12 Duphar International Research B.V. 8,9-anellated-1,2,3,4-tetrahydro-β-carboline derivatives
US5491168A (en) * 1991-08-27 1996-02-13 Uniroyal Chemical Company, Inc. Synergistic insecticidal compositions
EP0620222A3 (fr) * 1993-04-14 1995-04-12 Lilly Co Eli Tétrahydro-bêta-carbolines.
US5631265A (en) 1994-03-11 1997-05-20 Eli Lilly And Company 8-substituted tetrahydro-beta-carbolines
US5861409A (en) * 1995-05-19 1999-01-19 Eli Lilly And Company Tetrahydro-beta-carbolines
US7595311B2 (en) * 2002-05-24 2009-09-29 Exelixis, Inc. Azepinoindole derivatives as pharmaceutical agents
TWI329111B (en) * 2002-05-24 2010-08-21 X Ceptor Therapeutics Inc Azepinoindole and pyridoindole derivatives as pharmaceutical agents
US20060235012A1 (en) * 2003-06-16 2006-10-19 Chroma Therapeutics Limited Carboline and betacarboline derivatives for use as hdac enzyme inhibitors
AR045843A1 (es) * 2003-10-03 2005-11-16 Solvay Pharm Bv Derivados de bencimidazolonas y quinazolinonas sustituidas con hidronopol como agonistas en receptores orl 1 humanos
DE10360792A1 (de) * 2003-12-23 2005-07-28 Grünenthal GmbH Spirocyclische Cyclohexan-Derivate
DE10360793A1 (de) * 2003-12-23 2005-07-28 Grünenthal GmbH Spirocyclische Cyclohexan-Derivate
EP1828195A2 (fr) * 2004-11-23 2007-09-05 PTC Therapeutics, Inc. Phenols substitues en tant qu'agents actifs inhibant la production de vegf
WO2006085651A1 (fr) * 2005-02-14 2006-08-17 Nsk Ltd. Roulement d'unite de moyeu
EP1747779A1 (fr) * 2005-07-28 2007-01-31 Laboratorios Del Dr. Esteve, S.A. Dérivés de tetrahydro-b-carboline comme ligands du récepteur 5-HT6
WO2007062175A2 (fr) 2005-11-21 2007-05-31 Amgen Inc. Antagonistes cxcr3
DE102006046745A1 (de) * 2006-09-29 2008-04-03 Grünenthal GmbH Gemischte ORL1/µ-Agonisten zur Behandlung von Schmerz

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004043967A1 (fr) * 2002-11-11 2004-05-27 Grünenthal GmbH Derives de cyclohexane spirocycliques
WO2006108565A1 (fr) * 2005-04-11 2006-10-19 Grünenthal GmbH Derives de cyclohexane spirocycliques permettant de traiter une dependance a une substance
WO2008009415A2 (fr) * 2006-07-18 2008-01-24 Grünenthal GmbH Dérivés hétéroaryliques substitués

Cited By (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9296743B2 (en) 2008-01-11 2016-03-29 Albany Molecular Research, Inc. (1-azinone)-substituted pyridoindoles
US9650378B2 (en) 2008-01-11 2017-05-16 Albany Molecular Research, Inc. (1-azinone)-substituted pyridoindoles
US8716308B2 (en) 2008-01-11 2014-05-06 Albany Molecular Research, Inc. (1-azinone)-substituted pyridoindoles
US8357705B2 (en) 2008-03-27 2013-01-22 Gruenenthal Gmbh Substituted cyclohexyldiamines
US8293758B2 (en) 2008-03-27 2012-10-23 Grunenthal Gmbh Substituted spirocyclic cyclohexane derivatives
US8835689B2 (en) 2008-03-27 2014-09-16 Grünenthal GmbH Substituted 4-aminocyclohexane derivatives
US9580386B2 (en) 2008-03-27 2017-02-28 Grünenthal Substituted 4-aminocyclohexane derivatives
US9403767B2 (en) 2008-03-27 2016-08-02 Gruenenthal Gmbh Substituted 4-aminocyclohexane derivatives
US8288430B2 (en) 2008-03-27 2012-10-16 Grunenthal Gmbh Spiro(5.5)undecane derivatives
US8288406B2 (en) 2008-03-27 2012-10-16 Gruenenthal Gmbh Hydroxymethylcyclohexylamines
US8629158B2 (en) 2009-07-01 2014-01-14 Albany Molecular Research, Inc. Azabicycloalkane-indole and azabicycloalkane-pyrrolo-pyridine MCH-1 antagonists, methods of making, and use thereof
US9073925B2 (en) 2009-07-01 2015-07-07 Albany Molecular Research, Inc. Azinone-substituted azabicycloalkane-indole and azabicycloalkane-pyrrolo-pyridine MCH-1 antagonists, methods of making, and use thereof
US8637501B2 (en) 2009-07-01 2014-01-28 Albany Molecular Research, Inc. Azinone-substituted azepino[b]indole and pyrido-pyrrolo-azepine MCH-1 antagonists, methods of making, and use thereof
US8618299B2 (en) 2009-07-01 2013-12-31 Albany Molecular Research, Inc. Azinone-substituted azapolycycle MCH-1 antagonists, methods of making, and use thereof
US8993765B2 (en) 2010-12-21 2015-03-31 Albany Molecular Research, Inc. Tetrahydro-azacarboline MCH-1 antagonists, methods of making, and uses thereof
US8697700B2 (en) 2010-12-21 2014-04-15 Albany Molecular Research, Inc. Piperazinone-substituted tetrahydro-carboline MCH-1 antagonists, methods of making, and uses thereof
US10323040B2 (en) 2014-02-27 2019-06-18 Gruenenthal Gmbh Process for the preparation of 5-fluorotryptophol
US10202345B2 (en) 2014-07-15 2019-02-12 Gruenenthal Gmbh Substituted azaspiro(4.5)decane derivatives
US10214520B2 (en) 2014-07-15 2019-02-26 Gruenenthal Gmbh Substituted azaspiro(4.5)decane derivatives

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BRPI0806796A2 (pt) 2011-09-13
EP2121689A1 (fr) 2009-11-25
ECSP099620A (es) 2009-10-30
AU2008217276B2 (en) 2012-08-23
IL200497A0 (en) 2010-04-29
CA2679166C (fr) 2016-01-19
US8404740B2 (en) 2013-03-26
ES2433205T3 (es) 2013-12-09
CN101622255B (zh) 2013-12-11
US20100048554A1 (en) 2010-02-25
IL200497A (en) 2014-02-27
DE102007009235A1 (de) 2008-09-18
RU2484092C2 (ru) 2013-06-10
ZA200906585B (en) 2010-06-30
JP5366832B2 (ja) 2013-12-11
HK1136828A1 (en) 2010-07-09
EP2121689B1 (fr) 2013-07-31
RU2009135072A (ru) 2011-03-27
AU2008217276A1 (en) 2008-08-28
CN101622255A (zh) 2010-01-06
KR101515795B1 (ko) 2015-04-29
PL2121689T3 (pl) 2013-12-31
MX2009008781A (es) 2009-08-24
CA2679166A1 (fr) 2008-08-28

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